GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysA in Methyloferula stellata AR4T

Align Diaminopimelate decarboxylase; DAP decarboxylase; DAPDC; EC 4.1.1.20 (characterized)
to candidate WP_026595549.1 A3OQ_RS0106185 type III PLP-dependent enzyme

Query= SwissProt::B4XMC6
         (405 letters)



>NCBI__GCF_000385335.1:WP_026595549.1
          Length = 376

 Score =  107 bits (268), Expect = 4e-28
 Identities = 110/373 (29%), Positives = 170/373 (45%), Gaps = 32/373 (8%)

Query: 14  PFYLYDFDKIKQAFLNYKEAFKGRKSLICYALKANSNLSILSLLAHLESGADCVSIGEIQ 73
           P  + D D ++  + ++ +A    +  I YA+KAN +  +LSLLA L S  D  S+ EI+
Sbjct: 17  PCMVLDLDVVRDNYFSFAKALPDTR--IFYAVKANPDPQVLSLLAELGSCFDTASVVEIE 74

Query: 74  RALKAGIKPYRIVFSGVGKSAFEIEQALKLNILFLNVESFMELKTIETIAQSLGIKARIS 133
           + L AG    RI F    K   +I +A  L +    V+   E++ I  +A      +++ 
Sbjct: 75  QVLAAGASADRISFGNTIKKERDIARAYALGVRLFAVDCEAEVEKIARVAPG----SKVF 130

Query: 134 IRINPNIDAKTHPYISTGLKENKFGVGEKEALEMFLWAKKSAFLEPVSVHFHIGSQLLDL 193
            RI  +      P         KFG     A  +   A  S  L    + FH+GSQ  D 
Sbjct: 131 CRILCDATGAEWPL------SRKFGCAPAMAPRVLEHAH-SLGLNAYGLSFHVGSQQRDP 183

Query: 194 EPIIEASQKVAKIAKSLIALGIDLRFFDVGGGIGVSY-ENEETIKLYDYAQGILNALQ-- 250
                A +  A+I + L   GI L+  ++GGG    Y  N   +K   Y Q I  +L+  
Sbjct: 184 RMWDGALKAAAEIFRDLAERGISLQMVNLGGGFPTKYLRNVPAVKA--YGQSIFKSLRKH 241

Query: 251 ---GLDLTIICEPGRSIVAESGELITQ-VLYEKKAQNK--RFVIVDAG-MNDFLRPSLYH 303
               +  TII EPGR +V  +G +  + VL  KK+     ++V +D G  N     +   
Sbjct: 242 FGNRIPETII-EPGRGMVGNAGIIEAEVVLISKKSDTDQVKWVYLDIGKFNGLAETTDEM 300

Query: 304 AKHAIRVITPSKGREISPCDVVGPVCESSDT-FLKDAHL--PELEPGDKIAIEKVGAYGS 360
            ++ I+       +E  PC + GP C+S D  + KD +L    LE G K+ IE  GAY +
Sbjct: 301 IRYPIKTAFDHDAKE--PCVLAGPSCDSVDVLYEKDPYLLPVSLEIGAKVLIEGTGAYTT 358

Query: 361 SMAS-QYNSRPKL 372
           + +S  +N  P L
Sbjct: 359 TYSSVGFNGFPPL 371


Lambda     K      H
   0.319    0.138    0.389 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 281
Number of extensions: 15
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 405
Length of database: 376
Length adjustment: 31
Effective length of query: 374
Effective length of database: 345
Effective search space:   129030
Effective search space used:   129030
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory